QA/QC in the Wastewater Laboratory. Steve Roberts Ohio EPA Division of Environmental Services 05/11/2016

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Transcription:

QA/QC in the Wastewater Laboratory Steve Roberts Ohio EPA Division of Environmental Services 05/11/2016

What is Quality Assurance? Per Standard Methods for the Examination of Water and Wastewater, 21 st Ed. Quality Assurance a definitive plan for laboratory operation that specifies the measures used to produce data of known precision and bias.

What is Quality Control? Per Standard Methods for the Examination of Water and Wastewater, 21 st Ed. Quality Control set of measures within a sample analysis methodology to assure that the process is in control.

Code of Federal Regulation 136.7: Quality Assurance and Quality Control Requires the use of suitable QA/QC procedures when analyzing compliance samples Most will be listed in the approved methods If they aren t, then refer to the equivalent EPA method If that fails, 136.7 lists the requirements

40 CFR 136.7 Twelve QC elements where suitable. Demonstration of capability Method detection limit study Lab reagent blank Lab fortified blank Matrix spike/matrix spike duplicate Internal standards/surrogate standards/tracers

40 CFR 136.7 Cont. Calibration/calibration verification/continuing calibration verification Control charts Corrective action QC acceptance criteria Definitions of preparatory and analytical batches Minimum frequency for conducting all QC elements

Demonstration of Capability Can vary from method to method Determination of linearity Analysis of QC and blank samples Method detection limit study

Method Detection Limit Study Estimate the detection limit for the method Spike reagent water at 1-5 times the EDL Process at least seven aliquots through the entire method Times the standard deviation of the measurements by the student s T value If the level of analyte in the sample was below the determined MDL or exceeds 10 times the MDL of the analyte in reagent water, do not report a value for the MDL. Repeat the study if it fails

MDL Study with 2015 MUR Requires analysis of both 7 spiked and 7 blank samples Both preparation and analysis of these samples must include at least three batches on three separate calendar dates If multiple instruments are used for the analysis, the study must be spread across all of them

2015 MUR MDL cont. Calculate both the MDL s and the MDL b If none of the blank aliquots provide a numerical result, the MDL b does not apply If some, but not all of the blank aliquots provide numerical results, the MDL b is set at the highest blank value Whichever MDL is greater (MDL b or MDL s ) will now be the initial MDL

2015 MUR MDL cont. During any quarter in which samples are being analyzed, prepare and analyze a minimum of two spiked blanks on each instrument, in separate batches if available Ensure that at least 7 spiked blanks and 7 method blanks are completed for the annual verification At least once per year, re-calculate MDL s and MDL b from the collected spiked blank and method blank results

Per batch QC Lab reagent blank Reagent water with the same preservatives and prep as a regular sample Lab fortified blank A sample of reagent water that has been spiked with the analyte/s of concern treated exactly as a regular sample

Per batch QC cont. Matrix spike/matrix spike duplicate/duplicate % Recovery = (MS results sample result) Known spike concentration X 100% Internal standards/surrogates/tracers Internal standards are primarily for organics and some metals analysis Surrogates are used for organics analysis Tracers are used for radiochemistry analysis

Calibration Initial calibration A minimum of three for linear curves A minimum of five for non-linear curves Calibration verification Frequency can vary

Control Charts Two types of charts are primarily used Accuracy charts Precision charts

% Recovery Example of an accuracy chart 120% COD Water: ACCURACY IPC 100 ppb 115% 110% 105% 100% 95% 90% 85% 80% DATE OF ANALYSIS daily avg LCL LWL historical UWL UCL

DAILY AVERAGE Example of a precision chart CHLORIDE Precision 14% 12% 10% 8% 6% 4% 2% 0% DATE OF ANALYSIS RPD CL historical average

Corrective Action Corrective action must be taken when data is out of control Examples: Check data for calculation/transcription error Check calibration standards against a second source or QCS If LFB fails, analyze a second If the second LFB fails, check against a secondary source or QCS If a LFM fails, check LFB. If the LFB is acceptable qualify the data for the LFM sample or use another method

Other 40 CFR 136.7 requirements QC acceptance criteria Check the individual methods Check the QCS certificate of analysis You may have to develop certain ones based on your data Definition of prep and analytical batches Lab and sample volume dependent

Quality Controls in Standard Methods Large QA/QC section in the front of the book Not all QC requirements are covered in the large QC section Check individual methods Check the beginning portion of each series of method.

Documentation Bench sheets Logbooks What should be written in logbooks? Temperature logs Laboratory Information Management Systems (LIMS)

Questions? Steve Roberts Division of Environmental Services 8955 East Main St. Reynoldsburg, OH 43068 614-644-4225 steven.roberts@epa.ohio.gov